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Immunodeficiency associated with FCN3 mutation and ficolin-3 deficiency
Lea Munthe-Fog, Tina Hummelshøj, Christian Honoré, Hans O Madsen, Henrik Permin,
Peter Garred
Afdeling for Klinisk Immunologi
152
Citationer (Scopus)
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Keyphrases
Immunodeficiency
100%
Ficolin-3
100%
FCN3
100%
White People
25%
Liver
25%
Serum Levels
25%
Heterozygosity
25%
Lung
25%
Complement System
25%
Complement Activation
25%
Recognition Molecule
25%
Recurrent Infection
25%
Frameshift mutation
25%
Lectin Pathway
25%
Terminal End
25%
Disease Allele
25%
Immunology and Microbiology
Ficolin
100%
Immunodeficiency
100%
Blood Level
25%
Heterozygosity
25%
Carboxy Terminal Sequence
25%
Complement Activation
25%
Complement System
25%
Gene Frequency
25%
Lectin Pathway
25%
Frameshift Mutation
25%
Biochemistry, Genetics and Molecular Biology
Ficolin
100%
Blood Level
25%
Heterozygosity
25%
C-Terminus
25%
Complement Activation
25%
Gene Frequency
25%
Lectin Pathway
25%
Complement System
25%
Frameshift Mutation
25%